Empagliflozin as a Potential Therapeutic Solution for Patients With Brugada Syndrome

Inclusion Criteria

1. Patients diagnosed with Brugada syndrome and aged 18-99 years with spontaneous type 1 ECG, normal structural heart and patent coronary artery
2. Obtain written informed consent for participation in the clinical trial

Exclusion Criteria

1. Individuals with type 1 ECG pattern only observed with fever-induced or drug-induced were excluded from this exploratory study.
2. Current or prior use of an SGLT2 inhibitor within 12 weeks before screening or randomization
3. Known allergy or hypersensitivity to any SGLT2 inhibitor
4. History of ketoacidosis
5. Symptomatic hypotension or systolic blood pressure <90 mmHg or >180 mmHg
6. Heart failure
7. Acute myocardial infarction
8. ALT or AST >3× ULN at screening
9. Impaired renal function (eGFR <20 mL/min/1.73 m² [MDRD]), requiring dialysis, or functioning kidney transplant at screening
10. Pregnancy, nursing, or planning pregnancy during the trial
11. Enrollment in another investigational drug or device study or completion of such a study within the last 30 days
12. Known poor adherence to clinic visits or prescribed medications
13. Medical conditions that may limit trial participation, including severe respiratory disease, history of cancer with metastasis in the past four years (excluding non-melanoma skin cancer), or recent alcohol/substance misuse

Trial protocol The initial dose will start at 10 mg empagliflozin once a day, with monthly follow-ups for dose titration based on ECG ST-segment morphology done in lead V1, V2 at 4th, 3rd and 2nd intercostal spaces (ICSs). Responder is defined as any one of lead with a decrease in J-point elevation ≥1 mm from baseline. Responders will continue receiving 10 mg empagliflozin once a day, while non-responders will have their dose increased to 25 mg once a day.

This study followed a structured clinical trial protocol, including Screening, Treatment, and Follow-up periods. Participants underwent assessments at five scheduled visits corresponding to weeks -4 (screening), 4, 8, 12 (treatment phase), and 16 (follow-up). Peripheral blood mononuclear cell，(PBMC) will be collected and send to Stanford lab for Induced pluripotent stem cell (iPCS) once patient is enrolled in this study. Key evaluations included body weight (BW), automated office blood pressure (AOBP), and 12-lead electrocardiography (ECG). Safety monitoring encompassed adverse event documentation and laboratory tests with 15ml blood sample, including complete blood count (CBC), liver function tests (AST/ALT), renal function tests (BUN/creatinine), urinalysis, glucose AC, HbA1c, and ketone measurements. These assessments were conducted at predefined time points to ensure comprehensive monitoring of treatment effects and safety throughout the study duration.

Endpoints

Efficacy Endpoint Maximal change of type 1 Brugada ECG pattern recording with lead V1 and V2 in 4th, 3rd, and 2nd ICSs. Change of type 1 Brugada ECG pattern was defined as maximal J point elevation minus baseline J point elevation in the same leads. The responder is defined as decreased ≥ 1mm of J point in any one of above 6 leads.

Safety Endpoint Adverse event (AE) will be monitored as trail protocol. Adverse event including hypotension, symptomatic hypotension, acute renal failure, hepatic injury, ketoacidosis, hypoglycemic events, urinary tract infections, genital infections, bone fractures, events leading to lower limb amputation.

A serious adverse event (SAE) is any adverse event that results in death, is life-threatening, necessitates hospitalization or prolongation of existing hospitalization, causes significant disability or incapacity, leads to congenital anomalies or birth defects, or is deemed medically significant, potentially requiring intervention to prevent serious outcomes.

In accordance with the study protocol, the hospital will provide professional medical care and consultation in the event of adverse reactions or harm resulting from the clinical trial. Any adverse events will be reported to the Institutional Review Board (IRB) as required, with continuous monitoring of other participants' responses. All tests conducted are routine hospital examinations and pose no psychological harm to participants. Participant rights and protections will be upheld in accordance with the informed consent agreement.